Jl. Bradley et al., MYELINATED NERVE-FIBER REGENERATION IN DIABETIC SENSORY POLYNEUROPATHY - CORRELATION WITH TYPE OF DIABETES, Acta Neuropathologica, 90(4), 1995, pp. 403-410
Observations were made on myelinated fibre regeneration in diabetic se
nsory polyneuropathy assessed in sural nerve biopsy specimens. These c
onfirmed that regenerative clusters initially develop within abnormall
y persistent Schwann cell;basal laminal tubes. The number of regenerat
ing fibres, identified by light microscopy, was found to decline in pr
oportion to the reduction in total myelinated fibre density. The relat
ive number of regenerating fibres was significantly greater in patient
s with insulin-dependent as compared with those with non-insulin-depen
dent diabetes after correction for age. There was a slight negative co
rrelation between the relative proportion of regenerating fibres and a
ge, but this was not statistically significant. The progressive reduct
ion in the number of regenerating fibres with declining total fibre de
nsity indicates that axonal regeneration fails with advancing neuropat
hy. The production of nerve growth factor (NGF) and NGF receptors by d
enervated Schwann cells is likely to be important for axonal regenerat
ion. To investigate whether the failure of axonal regeneration could b
e related to a lack of NGF receptor production by Schwann cells, we ex
amined the expression of p75 NGF receptors by Bungner bands immunocyto
chemically. In comparison with other types of peripheral neuropathy, p
75 NGF receptor expression appeared to take place normally. It is conc
luded that failure of axonal regeneration constitutes an important com
ponent in diabetic neuropathy. Its explanation requires further invest
igation.